A novel hydride rearrangement of the acetal group of tetraacetal tetraoxa-cages mediated by Lewis acids

dc.citation.epage548en_US
dc.citation.spage547en_US
dc.citation.woscount9en_US
dc.contributor.authorWu, HJen_US
dc.contributor.authorChern, JHen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2019-04-02T06:00:19Z
dc.date.available2019-04-02T06:00:19Z
dc.date.issued1997-03-21en_US
dc.description.abstractTreatment of tetraoxa-cages 1a-f with Lewis acids such as TlC4, AlCl3, BF3 . OEt(2) and MeSO(3)H in dichloromethane at 25 degrees C gives the rearrangement products 2a-f in 90% yields regioselectively and stereoselectively; a novel hydride rearrangement of the acetal group of tetraacetal tetraoxa-cages mediated by Lewis acids.en_US
dc.identifier.doi10.1039/a607403ken_US
dc.identifier.issn1359-7345en_US
dc.identifier.journalCHEMICAL COMMUNICATIONSen_US
dc.identifier.urihttp://dx.doi.org/10.1039/a607403ken_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/149476
dc.identifier.wosnumberWOS:A1997WQ73300019en_US
dc.language.isoen_USen_US
dc.titleA novel hydride rearrangement of the acetal group of tetraacetal tetraoxa-cages mediated by Lewis acidsen_US
dc.typeArticleen_US

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